Canonical Allele Identifier: CA2690635339

Gene: ROR2

Linked Data

• gnomAD v4: 9-91757217-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757217G>C , CM000671.2:g.91757217G>C	GRCh38
NC_000009.11:g.94519499G>C , CM000671.1:g.94519499G>C	GRCh37
NC_000009.10:g.93559320G>C	NCBI36
NG_008089.1:g.197946C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.463+55C>G MANE Select	ENSP00000364860.3:n.463+55C>G
ENST00000375708.3:c.463+55C>G	ENSP00000364860.3:n.463+55C>G
ENST00000375715.5:c.43+55C>G	ENSP00000364867.1:n.43+55C>G
ENST00000548585.2:n.172+212C>G
ENST00000550066.5:n.931+55C>G
NM_004560.3:c.463+55C>G	NP_004551.2:n.463+55C>G
XM_005252008.3:c.43+55C>G	XP_005252065.1:n.43+55C>G
XM_006717121.2:c.43+55C>G	XP_006717184.1:n.43+55C>G
XM_011518721.1:c.43+55C>G	XP_011517023.1:n.43+55C>G
NM_001318204.1:c.463+55C>G	NP_001305133.1:n.463+55C>G
XM_005252008.4:c.43+55C>G	XP_005252065.1:n.43+55C>G
XM_006717121.3:c.43+55C>G	XP_006717184.1:n.43+55C>G
XM_017014762.1:c.454+55C>G	XP_016870251.1:n.454+55C>G
XM_017014763.1:c.43+55C>G	XP_016870252.1:n.43+55C>G
XR_001746315.1:n.706+55C>G
NM_004560.4:c.463+55C>G MANE Select	NP_004551.2:n.463+55C>G
NM_001318204.2:c.463+55C>G	NP_001305133.1:n.463+55C>G